PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of Pex12p

Molecular and Cellular Biology

Volumn 18, Issue 7, 1998, Pages 4324-4336

  Okumoto, Kanji ^a   Shimozawa, Nobuyuki ^b   Kawai, Atsusi ^a   Tamura, Shigehiko ^a   Tsukamoto, Toshiro ^c   Osumi, Takashi ^c   Moser, Hugo ^e   Wanders, Ronald J A ^f   Suzuki, Yasuyuki ^b   Kondo, Naomi ^b   Fujiki, Yukio ^a,d  

^a KYUSHU UNIVERSITY   (Japan)

^b GIFU UNIVERSITY   (Japan)

^c UNIVERSITY OF HYOGO   (Japan)

^d JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^e JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; EPITOPE; GREEN FLUORESCENT PROTEIN; MEMBRANE PROTEIN; ZINC FINGER PROTEIN;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CELL MUTANT; CHO CELL; CONTROLLED STUDY; CYTOPLASM; CYTOSOL; FIBROBLAST; GENETIC ANALYSIS; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PEROXISOME; POINT MUTATION; PRIORITY JOURNAL; ZELLWEGER SYNDROME;

ANIMALIA; LATEOLABRAX JAPONICUS;

EID: 0031862579     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.18.7.4324     Document Type: Article

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